Pages that link to "Q42006352"

The following pages link to A large deletion of the long arm of chromosome No. 4 in a child with limb abnormalities (Q42006352):

Displaying 23 items.

• Holt-Oram syndrome is a genetically heterogeneous disease with one locus mapping to human chromosome 12q (Q28246332) (← links)
• Deletion from the long arm of chromosome 4 (46,XX,4q-) associated with congenital anomalies (Q33585573) (← links)
• A patient with congenital anomalies and a deletion of the long arm of the long arm of chromosome 4 [46,XY,del(4)(q31)] (Q33586512) (← links)
• The Holt-Oram syndrome (Q33597087) (← links)
• A terminal deletion of the long arm of chromosome 4 [46,XX,del(4)(q33)] in an infant with phenotypic features of Williams syndrome. (Q33673791) (← links)
• Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature. (Q33828795) (← links)
• Interstitial deletion 4q32-34 with ulnar deficiency: 4q33 may be the critical region in 4q terminal deletion syndrome (Q34176481) (← links)
• Sleeping giants: emerging roles for the fat cadherins in health and disease (Q34347563) (← links)
• A large deletion of chromosome no. 1 (46,XY,1?--) (Q34633110) (← links)
• Dominant piebald trait in a retarded child with a reciprocal translocation and small intercalary deletion. (Q35570791) (← links)
• Child with multiple anomalies and a group B(4-5) long arm deletion (Bq-). (Q39492771) (← links)
• Renal and urinary tract abnormalities associated with chromosome aberrations. (Q39699394) (← links)
• Cytogenetics and Genetics (Q39971429) (← links)
• Partial trisomy 4q due to familial 2/4 translocation (Q41518823) (← links)
• Identification of variants in the 4q35 gene FAT1 in patients with a facioscapulohumeral dystrophy-like phenotype (Q41536718) (← links)
• Deletion (4)(q33—>qter): A Case Report and Review of the Literature (Q41649395) (← links)
• A complex chromosomal rearrangement with formation of a ring 4 (Q42243576) (← links)
• Clinical and genomic characterization of distal duplications and deletions of chromosome 4q: study of two cases and review of the literature (Q51922364) (← links)
• A gene for Holt–Oram syndrome maps to the distal long arm of chromosome 12 (Q57199552) (← links)
• Holt-Oram syndrome (Q66927325) (← links)
• The partial 4q monosomy. Report of a 5-year-old boy with deletion 4q31.3 leads to 4qter (Q70450417) (← links)
• Partial monosomy of long arm of chromosome 4 due to interstitial deletion (Q71184973) (← links)
• Prenatal diagnosis of a maternal 7.22-Mb deletion at chromosome 4q32.2q32.3 by SNP array (Q92063371) (← links)